Canonical Allele Identifier: CA2216947181

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189223T= , CM000678.2:g.31189223T=	GRCh38
NC_000016.9:g.31200544T= , CM000678.1:g.31200544T=	GRCh37
NC_000016.8:g.31108045T=	NCBI36
NG_012889.2:g.14092T= , LRG_655:g.14092T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.933T= MANE Select	ENSP00000254108.8:p.Ile311=
ENST00000254108.11:c.933T=	ENSP00000254108.7:p.Ile311=
ENST00000380244.7:c.930T=	ENSP00000369594.3:p.Ile310=
ENST00000474990.5:n.227T=
ENST00000487509.6:n.4108T=
ENST00000564766.1:n.757T=
ENST00000566605.5:c.*106T=	ENSP00000455073.1:n.*106T=
ENST00000568685.1:c.936T=	ENSP00000455282.1:p.Ile312=
ENST00000568901.2:n.307T=
NM_001170634.1:c.930T=	NP_001164105.1:p.Ile310=
NM_001170937.1:c.921T=	NP_001164408.1:p.Ile307=
NM_004960.3:c.933T= , LRG_655t1:c.933T=	NP_004951.1:p.Ile311=
NR_028388.2:n.1003T=
XM_005255233.3:c.318T=	XP_005255290.1:p.Ile106=
XM_011545781.1:c.927T=	XP_011544083.1:p.Ile309=
XM_011545782.1:c.318T=	XP_011544084.1:p.Ile106=
XM_005255233.5:c.318T=	XP_005255290.1:p.Ile106=
XM_011545782.2:c.318T=	XP_011544084.1:p.Ile106=
XM_024450221.1:c.924T=	XP_024305989.1:p.Ile308=
NM_004960.4:c.933T= MANE Select	NP_004951.1:p.Ile311=